Development and Developmental Disorders of the Brain Stem
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-26098-8_7
Reference604 articles.
1. Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C et al (1997) A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nat Genet 15:157–164
2. Acampora D, Gulisano M, Broccoli V, Simeone A (2001) Otx genes in brain morphogenesis. Prog Neurobiol 64:69–95
3. Aicardi J (1998) Diseases of the nervous system in childhood, 2nd edn. Mac Keith, London
4. Alasti F, Sadeghi A, Sanati MH, Farhadi M, Stollar E, Somers T, Van Camp G (2008) A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family. Am J Hum Genet 82:982–991
5. Alaynick WA, Jessell TM, Pfaff SL (2011) SnapShot: spinal cord development. Cell 146:178–178
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